Question 1

What does it detect?

Accepted Answer

Down syndrome (Trisomy 21). Edwards syndrome (Trisomy 18). Patau syndrome (Trisomy 13). Some disorders related to the sex chromosomes (X and Y).

Question 2

Features:

Accepted Answer

Non-invasive It is done by taking a sample from the mother's blood, making it safer compared to surgical tests. Accurate Results It is characterized by an accuracy of up to 99% in detecting certain genetic abnormalities, especially Down syndrome. Done Early It can be performed early in pregnancy, typically starting from the 10th week.

Question 3

Recommended for:

Accepted Answer

Women at increased risk of genetic disorders due to age (35 years or older). Women with a family history of genetic abnormalities. Women who have had abnormal results in routine pregnancy tests.

Question 4

Optimal timing:

Accepted Answer

Typically between the 10th and 13th weeks of pregnancy. It can be performed early in pregnancy to help parents obtain accurate information about the health of the fetus, especially regarding the detection of certain genetic abnormalities like Down syndrome. This test is done using a simple blood sample from the mother, and it is recommended to be done during this early period to ensure accurate results and provide time for making necessary decisions based on the outcomes.

Question 5

Preparations:

Accepted Answer

No special preparation is required. It does not require fasting or any specific preparations before the test. It is always recommended to consult a specialist doctor before undergoing the test to obtain detailed information and ensure that the test is appropriate for your condition and pregnancy circumstances.

Question 6

Steps:

Accepted Answer

Purchase the service by selecting the appropriate provider below. Our medical team will contact you and may ask you to provide the necessary information about the patient's health and the address where the sample will be collected. Follow-up on the results: After the test is done, the medical team will review and analyze the results. Sending medical reports: The medical reports will be sent to you. Consulting with the doctor: Based on the results, the doctor may contact the patient or family to discuss the results and possible medical recommendations.

Question 7

Frequently Asked Questions (FAQs)

Accepted Answer

Is the genetic test safe for the mother and the fetus? Yes, the non-invasive genetic test is completely safe for both the mother and the fetus. It only requires a blood sample from the mother and does not affect the pregnancy in any way. When will I get the results? The results are usually ready within 5 to 10 business days, and they will be sent to you via email or through direct communication. Can the results be trusted? The genetic test (NIPT) is highly accurate, with an accuracy rate of up to 99% for detecting certain genetic abnormalities, and it is highly reliable in assessing pregnancy-related risks. Does the test cover all genetic disorders? The genetic test (NIPT) covers some of the most common genetic disorders such as Down syndrome and Edwards syndrome. If you need more detailed tests, you can talk to your doctor to discuss additional tests. What is the cost of the at-home genetic test? Does it include the medical team's visit fees? The cost of the test varies based on the package and services required. It includes the test fees and the fees for the medical team’s visit to take the sample. We provide you with a comprehensive breakdown of the costs. Is support provided if the results are abnormal? Yes, we offer full support in case the results are abnormal. Specialized medical consultations will be provided to help you understand the results and take the appropriate steps. How is the confidentiality of the results maintained? We adhere to the highest standards of confidentiality. The test results are securely stored and are only sent to you through trusted channels.

Non-Invasive Prenatal Test (NIPT) - Non-Invasive Prenatal Testing (NIPT)